Researchclopedia
Research
Researchers
Institutions
Topics
Submit
About
Search...
⌘
K
Command Palette
Search for a command to run...
Back to research
Exome Sequencing Reveals De Novo WDR45 Mutations Causing a Phenotypically Distinct, X-Linked Dominant Form of NBIA
2012
358 citations
Journal Article
bronze Open Access
Field-Weighted Citation Impact:
18.59
Exome Sequencing Reveals De Novo WDR45 Mutations Causing a Phenotypically Distinct, X-Linked Dominant Form of NBIA | Researchclopedia
·
Helmholtz Zentrum München
Lynn Sanford
·
Oregon Health & Science University
Esther Meyer
·
Great Ormond Street Hospital
Eleanna Kara
·
National Hospital for Neurology and Neurosurgery
Stephan M. Cuno
·
Helmholtz Zentrum München
Sami I. Harik
·
University of Arkansas for Medical Sciences
Vasuki Dandu
·
University of Arkansas for Medical Sciences
Nardo Nardocci
Giovanna Zorzi
Todd Dunaway
·
University of Tulsa
Mark A. Tarnopolsky
·
McMaster University Medical Centre
Steven A. Skinner
·
Greenwood Genetic Center
Steven J. Frucht
·
Icahn School of Medicine at Mount Sinai
Era Hanspal
·
Albany Medical Center Hospital
Connie Schrander‐Stumpel
·
Maastricht University Medical Centre
Delphine Héron
·
Sorbonne Université
Cyril Mignot
·
Sorbonne Université
Barbara Garavaglia
·
Fondazione IRCCS Istituto Neurologico Carlo Besta
Kailash P. Bhatia
·
National Hospital for Neurology and Neurosurgery
John Hardy
·
National Hospital for Neurology and Neurosurgery
Tim M. Strom
·
Helmholtz Zentrum München
Nathalie Boddaert
·
Hôpital Necker-Enfants Malades
Henry Houlden
·
National Hospital for Neurology and Neurosurgery
Manju A. Kurian
·
Great Ormond Street Hospital
Thomas Meitinger
·
Helmholtz Zentrum München
Holger Prokisch
·
Helmholtz Zentrum München
Susan J. Hayflick
·
Oregon Health & Science University